Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP31372.RAQKrzJGdS0FE2368HPr3mI8gLjIGqhfeeaUGfCQRJTsI130_assertion> ?p ?o ?g. }
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- NP31372.RAQKrzJGdS0FE2368HPr3mI8gLjIGqhfeeaUGfCQRJTsI130_assertion type Assertion NP31372.RAQKrzJGdS0FE2368HPr3mI8gLjIGqhfeeaUGfCQRJTsI130_head.
- NP31372.RAQKrzJGdS0FE2368HPr3mI8gLjIGqhfeeaUGfCQRJTsI130_assertion description "[TBX15 mutations cause craniofacial dysmorphism, hypoplasia of scapula and pelvis, and short stature in Cousin syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP31372.RAQKrzJGdS0FE2368HPr3mI8gLjIGqhfeeaUGfCQRJTsI130_provenance.
- NP31372.RAQKrzJGdS0FE2368HPr3mI8gLjIGqhfeeaUGfCQRJTsI130_assertion evidence source_evidence_curated NP31372.RAQKrzJGdS0FE2368HPr3mI8gLjIGqhfeeaUGfCQRJTsI130_provenance.
- NP31372.RAQKrzJGdS0FE2368HPr3mI8gLjIGqhfeeaUGfCQRJTsI130_assertion SIO_000772 19068278 NP31372.RAQKrzJGdS0FE2368HPr3mI8gLjIGqhfeeaUGfCQRJTsI130_provenance.
- NP31372.RAQKrzJGdS0FE2368HPr3mI8gLjIGqhfeeaUGfCQRJTsI130_assertion wasDerivedFrom ctd_human-20130708 NP31372.RAQKrzJGdS0FE2368HPr3mI8gLjIGqhfeeaUGfCQRJTsI130_provenance.
- NP31372.RAQKrzJGdS0FE2368HPr3mI8gLjIGqhfeeaUGfCQRJTsI130_assertion wasGeneratedBy ECO_0000218 NP31372.RAQKrzJGdS0FE2368HPr3mI8gLjIGqhfeeaUGfCQRJTsI130_provenance.